A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401156



Internal ID22459026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38592683..38592733hg38UCSC Ensembl
chr20:37221326..37221376hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951411
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401156
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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